Ammonia → {[(2R)-oxolan-2-yl]methyl}thiourea

HRID 78513

반응식

HRID 78513 반응식
[O:1]1[CH2:5][CH2:4][CH2:3][C@@H:2]1[CH2:6][NH2:7].C([N:10]([CH2:13]C)CC)C.C(=S)=[S:16].OO.N.CO>O1CCCC1.O>[O:1]1[CH2:5][CH2:4][CH2:3][C@@H:2]1[CH2:6][NH:7][C:13]([NH2:10])=[S:16]

참가 물질

9

실험 절차

To a 0° C. solution of (R)-(tetrahydrofuran-2-yl)methanamine (5.0 g, 49.5 mmol) and triethylamine (690 uL, 4.95 mmol) in tetrahydrofuran (100 mL) was added carbon disulfide (5.65 g, 74.3 mmol). Stirring was continued for 0.5 hour followed by the dropwise addition of 30% hydrogen peroxide (5.6 g, 49.5 mmol) so that the temperature was maintained below 40° C. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic extract was dried (Na2SO4), filtered and concentrated to afford an oil. The residue was dissolved in tetrahydrofuran, and treated with 7 N ammonia in methanol (14.3 mL, 100 mmol). The precipitate was collected by filtration and washed with water to afford the title compound.

후처리

  1. temperaturewas maintained below 40° C
  2. extractionextracted with ethyl acetate
  3. extractionThe organic extract
  4. dry with materialwas dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customto afford an oil
  8. filtrationThe precipitate was collected by filtration
  9. washwashed with water

출처 및 근거

ORD 기록
ord-ab61ef12de984805b7afab8d21846160
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841334B2

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